3gqf | pdb_00003gqf
From Proteopedia
Structural and Biophysical Properties of the Pathogenic SOD1 Variant H46R/H48Q
Disease
Known disease associated with this structure: Amyotrophic lateral sclerosis, due to SOD1 deficiency OMIM:[147450]
About this Structure
3GQF is a 6 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Wed Jun 17 20:16:12 2009
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Superoxide dismutase
- Hart, P J.
- Schuermann, J P.
- Winkler, D D.
- Acetylation
- Amyotrophic lateral sclerosis
- Antioxidant
- Copper
- Cytoplasm
- Disease mutation
- Disulfide bond
- Familial amyotrophic lateral sclerosis mutant
- Human cu-zn superoxide dismutase
- Metal-binding
- Oxidoreductase
- Phosphoprotein
- Superoxide acceptor
- Ubl conjugation
- Zinc
